采用缝合法建立小鼠尾椎椎间盘退变伴尾环模型。

Q1 Health Professions
Wei Xie, Zemao Huang, Ziyang Huang, Deqing Luo, Zhangxin Chen, Li Xie, Lingqi Zhu, Hui Liu, Kejian Lian, Paolo Alberton, Denitsa Docheva, Dasheng Lin
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引用次数: 0

摘要

背景:椎间盘退变(IDD)是常见的退行性疾病之一。由于伦理约束,很难获得充分的人体研究,因此利用IDD动物模型对阐明该病的发病机制和治疗机制非常重要。方法:选择32只2月龄大鼠进行手术建立尾骨IDD模型。切除尾远端尾部(第17尾椎外)和尾8尾椎上方一小块皮肤,屈折后将两个切口合拢,缝合固定。分别于术后0、6、12周采用微计算机断层扫描(μCT)和磁共振成像(MRI)评估椎间盘高度和信号强度。采用苏木精和伊红(HE)、红素O-Fast Green和免疫组化染色,对IVDs的整体组织形态、细胞分布和密度、细胞外基质进行评估。结果:实验组小鼠术后全部成活,无创面感染、尾坏死、缝线脱落等并发症。实验结果表明,该缝合方法可以成功启动IDD。通过控制尾环内ivd的弯曲角度,可以诱导不同程度的IDD;然而,为了一致性,应在相同的弯曲角度和循环周期下获得组织学和影像学结果。结论:该IDD模型是研究退行性IVD病因及治疗的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A mouse coccygeal intervertebral disc degeneration model with tail-looping constructed using a suturing method.

Backgroud: Intervertebral disc degeneration (IDD) is one of the common degenerative diseases. Due to ethical constraints, it is difficult to obtain sufficient research on humans, so the use of an animal model of IDD is very important to clarify the pathogenesis and treatment mechanism of the disease.

Methods: In this study, thirty 2-month-old mice were selected for operation to establish a coccygeal IDD model. The distal tail portion of the tail (beyond the 17th coccygeal vertebra) and a small piece of skin above the 8th coccygeal vertebra were excised, and the two incisions were brought together after flexion, and secured with sutures. The heights and signal intensities of the intervertebral discs (IVDs) were assessed using microcomputed tomography (μCT) and magnetic resonance imaging (MRI) at 0, 6, 12 weeks postoperatively. The overall tissue morphology, cell distribution and density, and extracellular matrix of the IVDs were also assessed using Hematoxylin and Eosin (HE), Safranin O-Fast Green and immunohistochemical staining.

Results: All mice in the experimental group survived after the operation, and there were no complications such as wound infection, tail necrosis and suture shedding. The experimental results demonstrated that the suturing method can successfully initiate IDD. Different severity levels of IDD can be induced by controlling the bending angle of the IVDs within the tail loop; however, for consistency, histologic and imaging results should be obtained at the same bending angle and looping period.

Conclusions: This IDD model is an effective method for studying the etiology and treatment of degenerative IVD disease.

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CiteScore
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